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80476-91-1

1-benzyl-4-(4-chloro-benzhydryl)-piperazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 80476-91-1 Structure

  • Basic information

    1. Product Name: 1-benzyl-4-(4-chloro-benzhydryl)-piperazine
    2. Synonyms: 1-benzyl-4-(4-chloro-benzhydryl)-piperazine
    3. CAS NO:80476-91-1
    4. Molecular Formula:
    5. Molecular Weight: 376.929
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80476-91-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-benzyl-4-(4-chloro-benzhydryl)-piperazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-benzyl-4-(4-chloro-benzhydryl)-piperazine(80476-91-1)
    11. EPA Substance Registry System: 1-benzyl-4-(4-chloro-benzhydryl)-piperazine(80476-91-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 80476-91-1(Hazardous Substances Data)

80476-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80476-91-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,4,7 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80476-91:
(7*8)+(6*0)+(5*4)+(4*7)+(3*6)+(2*9)+(1*1)=141
141 % 10 = 1
So 80476-91-1 is a valid CAS Registry Number.

80476-91-1Relevant articles and documents

Discriminating non-ylidic carbon-sulfur bond cleavages of sulfonium ylides for alkylation and arylation reactions

Fang, Jing,Li, Ting,Ma, Xiang,Sun, Jiuchang,Cai, Lei,Chen, Qi,Liao, Zhiwen,Meng, Lingkui,Zeng, Jing,Wan, Qian

supporting information, p. 288 - 292 (2021/07/25)

A sulfonium ylide participated alkylation and arylation under transition-metal free conditions is described. The disparate reaction pattern allowed the separate activation of non-ylidic S-alkyl and S-aryl bond. Under acidic conditions, sulfonium ylides serve as alkyl cation precursors which facilitate the alkylations. While under alkaline conditions, cleavage of non-ylidic S-aryl bond produces O-arylated compounds efficiently. The robustness of the protocols were established by the excellent compatibility of wide variety of substrates including carbohydrates.

OPTICALLY ACTIVE CARBAMATES, PROCESS FOR PREPARATION THEREOF AND USE THEREOF AS PHARMACEUTICAL INTERMEDIATES

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Page/Page column 24-25, (2008/06/13)

The present invention is related to l-[(4-chlorophenyl)-phenylmethyl]-4-(2,2,2-trichloroethoxycarbonyl)-piperazine of the Formula (IV) and optically isomers thereof, process for preparation thereof and the use of the compound of the Formula (IV) in the preparation of l-(4-chlorophenyl)-phenylmethyl-piperazine and optical isomers and salts thereof. l-(4-chlorophenyl)-phenylmethyl-piperazine and optical isomers thereof are important intermediates in the preparation of non-sedating antihistamine-type active pharmaceutical ingredients.

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